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Circulation. Cardiovascular genetics

Showing results (321-330 of 961) with videos related to

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Circulation. Cardiovascular Genetics|December 25, 2009
Ethical challenges encountered in genomic researchPatricia A Roche
Circulation. Cardiovascular Genetics|December 25, 2009
Genome-wide association scan identifies variants near Matrix Metalloproteinase (MMP) genes on chromosome 11q21-22 strongly associated with serum MMP-1 levelsYu-Ching Cheng, Wen-Hong L Kao, Braxton D Mitchell, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Proteomics, metabolomics, and immunomics on microparticles derived from human atherosclerotic plaquesManuel Mayr, David Grainger, Ursula Mayr, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Desmoglein-2 and desmocollin-2 mutations in dutch arrhythmogenic right ventricular dysplasia/cardiomypathy patients: results from a multicenter studyZahurul A Bhuiyan, Jan D H Jongbloed, Jasper van der Smagt, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Comprehensive desmosome mutation analysis in north americans with arrhythmogenic right ventricular dysplasia/cardiomyopathyA Dénise den Haan, Boon Yew Tan, Michelle N Zikusoka, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Distinct early signaling events resulting from the expression of the PRKAG2 R302Q mutant of AMPK contribute to increased myocardial glycogenKaralyn D Folmes, Anita Y M Chan, Debby P Y Koonen, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Functional variant disrupts insulin induction of USF1: mechanism for USF1-associated dyslipidemiasJussi Naukkarinen, Emma Nilsson, Heikki A Koistinen, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Genetic ancestry, population admixture, and the genetic epidemiology of complex diseaseDaniel L Dries
Circulation. Cardiovascular Genetics|December 25, 2009
SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndromeVincent Probst, Arthur A M Wilde, Julien Barc, et al.
Circulation. Cardiovascular Genetics|October 5, 2017
Diminished <i>PRRX1</i> Expression Is Associated With Increased Risk of Atrial Fibrillation and Shortening of the Cardiac Action PotentialNathan R Tucker, Elena V Dolmatova, Honghuang Lin, et al.
Pageof 97

Showing results (321-330 of 961) with videos related to

Sort By:
Pageof 97
Circulation. Cardiovascular Genetics|December 25, 2009
Ethical challenges encountered in genomic researchPatricia A Roche
Circulation. Cardiovascular Genetics|December 25, 2009
Genome-wide association scan identifies variants near Matrix Metalloproteinase (MMP) genes on chromosome 11q21-22 strongly associated with serum MMP-1 levelsYu-Ching Cheng, Wen-Hong L Kao, Braxton D Mitchell, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Proteomics, metabolomics, and immunomics on microparticles derived from human atherosclerotic plaquesManuel Mayr, David Grainger, Ursula Mayr, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Desmoglein-2 and desmocollin-2 mutations in dutch arrhythmogenic right ventricular dysplasia/cardiomypathy patients: results from a multicenter studyZahurul A Bhuiyan, Jan D H Jongbloed, Jasper van der Smagt, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Comprehensive desmosome mutation analysis in north americans with arrhythmogenic right ventricular dysplasia/cardiomyopathyA Dénise den Haan, Boon Yew Tan, Michelle N Zikusoka, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Distinct early signaling events resulting from the expression of the PRKAG2 R302Q mutant of AMPK contribute to increased myocardial glycogenKaralyn D Folmes, Anita Y M Chan, Debby P Y Koonen, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Functional variant disrupts insulin induction of USF1: mechanism for USF1-associated dyslipidemiasJussi Naukkarinen, Emma Nilsson, Heikki A Koistinen, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Genetic ancestry, population admixture, and the genetic epidemiology of complex diseaseDaniel L Dries
Circulation. Cardiovascular Genetics|December 25, 2009
SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndromeVincent Probst, Arthur A M Wilde, Julien Barc, et al.
Circulation. Cardiovascular Genetics|October 5, 2017
Diminished <i>PRRX1</i> Expression Is Associated With Increased Risk of Atrial Fibrillation and Shortening of the Cardiac Action PotentialNathan R Tucker, Elena V Dolmatova, Honghuang Lin, et al.
Pageof 97